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EOPA Arterial Cannula - Bangladesh Medical Device Registration

Access comprehensive regulatory information for EOPA Arterial Cannula in the Bangladesh medical device market through Pure Global AI's free database. This C medical device is manufactured by MedtronicPerfusionSystemUSAforMedtronicInc in USA. The device was registered on September 02, 2020.

This page provides complete registration details including registration ID (467-6750-2020), manufacturer information and country of origin (USA), authorized representative (Medtronic Bangladesh Pvt. Ltd., Level 6, Shanta Western Tower, 186, Gulshan Tejgaon Link Road, Dhaka), risk classification, and regulatory compliance data from the official Bangladesh medical device database. Pure Global AI offers free access to Bangladesh DGDA's medical device registry, helping global MedTech companies navigate Bangladesh regulations efficiently.

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Bangladesh DGDA Official Data
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EOPA Arterial Cannula
Bangladesh Medical Device Registration
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Device Classification
Risk Class
C
Product Name
EOPA Arterial Cannula
Registration Information
Registration ID
467-6750-2020
Registration Date
September 02, 2020
Analysis ID
ad166c5ed8a8edddec227a040f966b4e